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. 2021 Nov 19;38(20):4659–4669. doi: 10.1093/bioinformatics/btab790

Table 3.

Open syncmer versus minimizer mappings for two versions of minimap2 on long-reads. We fix parameters (k,s,t,w)=(15,11,3,9) so the density is 1/5 for both seeding methods

Long-read dataset Reference |OSM¯| (mapQ) |MOS¯| (mapQ) |OS| |M| Total no. of reads % increase in mapped reads
E.coli W (bc1087) E.coli W (bc1087) 312 (21.56) 102 (11.57) 194 455 194 245 196 901 0.108
E.coli K12 (bc1106) E.coli W (bc1087) 548 (20.30) 187 (11.33) 220 459 220 098 226 906 0.164
K.pneumoniae (bc1074) E.coli W (bc1087) 11 434 (19.80) 3679 (12.10) 143 724 135 969 251 838 5.70
Downsampled human ONT (rel3) Human—CHM13 370 (3.53) 103 (2.52) 37 819 37 552 51 210 0.711
Downsampled human ONT (rel3) Mouse—GRCm38 2467 (2.32) 1005 (1.90) 19 214 17 752 51 210 8.23

Note: OS is the subset of reads successfully mapped using open syncmers, and M similarly for minimizers. OSM¯ is the set of reads which are uniquely mapped by open syncmers, and MOS¯ are reads uniquely mapped by minimizers. The average mapQ outputted by minimap2 within the set is presented as well (Section 5.2).